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STERIS 4085 Surgical Table (REF ST013701)Recalls & reported problems

Steris Corporation · The STERIS 4085 Table Battery Line with TLT Pads SS Cover accommodates virtually all patients with generous weight and height ranges and provides outstanding access for C-Arm, permitting high quality images crucial to cardiothoracic, Orthopedic and neurosurgical procedures. · Class 1

Adverse event reports
6
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00724995154813), received between Feb 17, 2022 and Dec 19, 2025 — classified as 6 malfunctions.

The most frequently reported specific device problem is “Smoking” (2 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 1 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 1 reportsNov 2025: 0 reportsDec 2025: 1 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Smoking2
  • Unintended Movement2
  • Electrical Shorting1
  • Use of Device Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions6

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

  • MalfunctionDec 19, 2025Unintended Movement; Unintended Movement

    THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THEIR 4085 SURGICAL TABLE BEGAN TO TILT WHILE IN THE SUPINE POSITION AND THE PATIENT SLID FORWARD. THE PROCEDURE WAS CANCELLED, AND THE PATIENT RECEIVED A CT SCAN AND IS DOING WELL. NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23850082 ↗
  • MalfunctionOct 23, 2025Unintended Movement; Unintended Movement

    THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, THEIR 4085 SURGICAL TABLE WAS COMMANDED TO LEVEL VIA THE HAND CONTROL, HOWEVER, THE TABLE MOVEMENT WENT LEFT TO RIGHT. THE PATIENT WAS TRANSFERRED TO ANOTHER TABLE, AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23369222 ↗
  • MalfunctionDec 8, 2023Smoking; Smoking

    THE USER FACILITY REPORTED THAT AT THE START OF A PATIENT PROCEDURE, THEIR 4085 SURGICAL TABLE EMITTED AN "ELECTRICAL" BURNING SMELL AND SMALL AMOUNT OF SMOKE. THE PATIENT WAS TRANSFERRED TO A DIFFERENT TABLE WHICH CAUSED A DELAY IN THE COMPLETION OF THE PROCEDURE. THE PROCEDURE WAS COMPLETED SUCCESSFULLY; NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18296962 ↗
  • MalfunctionMay 2, 2023Use of Device Problem; Use of Device Problem

    THE USER FACILITY REPORTED THAT AT THE END OF A PATIENT PROCEDURE THEIR 4085 SURGICAL TABLE WAS STUCK IN TRENDELENBURG POSITION AS THE TABLE WAS NOT RESPONDING TO THE COMMANDS FROM THE MAIN OR BACKUP HAND CONTROLS. NO REPORT OF INJURY OR PROCEDURE DELAY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16855737 ↗
  • MalfunctionMar 22, 2023Smoking; Smoking

    THE USER FACILITY REPORTED THAT THEIR 4085 SURGICAL TABLE WAS EMITTING SMOKE. A PATIENT WAS NOT ON THE TABLE AT THE TIME OF THE REPORTED EVENT. NO REPORT OF INJURY. REPORT OF PROCEDURE DELAYS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16590608 ↗
  • MalfunctionFeb 17, 2022Electrical Shorting; Electrical Shorting

    THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THEIR 4085 SURGICAL TABLE BEGAN EMITTING SMOKE. THE PROCEDURE CONTINUED AND WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY OR PROCEDURE DELAY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13551001 ↗

Other TABLE, OPERATING-ROOM, AC-POWERED devices

All TABLE, OPERATING-ROOM, AC-POWERED devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.